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[ CAS No. 53981-38-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 53981-38-7
Chemical Structure| 53981-38-7
Structure of 53981-38-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 53981-38-7 ]

CAS No. :53981-38-7 MDL No. :MFCD00730969
Formula : C9H11NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :LCOFMNJNNXWKOC-UHFFFAOYSA-N
M.W : 149.19 Pubchem ID :4961957
Synonyms :

Calculated chemistry of [ 53981-38-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.3
TPSA : 35.25 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.56 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.65
Log Po/w (XLOGP3) : 0.92
Log Po/w (WLOGP) : 1.14
Log Po/w (MLOGP) : 1.14
Log Po/w (SILICOS-IT) : 1.63
Consensus Log Po/w : 1.3

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.75
Solubility : 2.66 mg/ml ; 0.0179 mol/l
Class : Very soluble
Log S (Ali) : -1.25
Solubility : 8.46 mg/ml ; 0.0567 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.36
Solubility : 0.654 mg/ml ; 0.00439 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.22

Safety of [ 53981-38-7 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 53981-38-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 53981-38-7 ]

[ 53981-38-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 53981-38-7 ]
  • [ 6290-49-9 ]
  • [ 730980-58-2 ]
  • [ 1035093-81-2 ]
YieldReaction ConditionsOperation in experiment
A mixture of 4-aminochromane hydrochloride (27.8 g, 0.15 mol) and aqueous sodium hydroxide (2N) was extracted with ethyl acetate and the organic layer dried (sodium sulfate) and evaporated to give racemic 4-aminochromane (14.2 g, 0.095 mol). To this was added methyl 2-methoxyacetate (10.94 g, 0.105 mol) and 2.5 g Novozym 435 (Aldrich Corp.) in tert-butyl methyl ether, and the mixture heated at reflux for 2 hours. A further addition of Novozym 435 (0.5 g) was made and heating continued until the reaction was complete as judged by hplc. Dichloromethane was added, the biocatalyst filtered off and the organic layer dried (sodium sulfate) and evaporated. The residue was dissolved in the minimum of dichloromethane, and ethanolic hydrochloric acid solution (8N) was added to give (4S)4-aminochromane hydrochloride which was filtered off, and the filtrate evaporated to give N-[(4R)4-chromanyl]-2-methoxyacetamide (8.2 g), mp. 109-112 C.
  • 2
  • [ 53981-38-7 ]
  • C9H9NO [ No CAS ]
  • [ 210488-55-4 ]
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